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CORRECTION article

Front. Pediatr., 30 March 2023
Sec. Children and Health
Volume 11 - 2023 | https://doi.org/10.3389/fped.2023.1183013

Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases

This article is a correction to:

  1. Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases

    1. Read original article
\r\nRui Liang,&#x;Rui Liang1,†Xuelan Chen,&#x;Xuelan Chen2,†Ying ZhangYing Zhang1Chak-Fun LawChak-Fun Law3Sijie YuSijie Yu2Jia JiaoJia Jiao2Qin YangQin Yang2Daoqi WuDaoqi Wu2Gaofu ZhangGaofu Zhang2Han ChenHan Chen2Mo WangMo Wang2Haiping YangHaiping Yang2Anshuo Wang \r\nAnshuo Wang2*
  • 1Department of Pediatrics, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China
  • 2Department of Nephrology, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing, China
  • 3Center for Biomedicine and Innovations, Faculty of Medicine, Macau University Science and Technology, Taipa, China

A Corrigendum on

Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases

By Liang R, Chen X, Zhang Y, Law C-F, Yu S, Jiao J, Yang Q, Wu D, Zhang G, Chen H, Wang M, Yang H and Wang A. (2023) Front. Pediatr. 10:1030191. doi: 10.3389/fped.2022.1030191

In the published article, the accession number mentioned in the Data Availability statement “HRA005507” was incorrect and didn't link to the database correctly. The correct Data Availability statement appears below.

Data availability statement

The data presented in the study are deposited in the GSA-Human repository, accession number HRA003933.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Keywords: COQ8B, coenzyme Q10, proteinuria, chronic kidney disease, FSGS, calcinosis

Citation: Liang R, Chen X, Zhang Y, Law C-F, Yu S, Jiao J, Yang Q, Wu D, Zhang G, Chen H, Wang M, Yang H and Wang A (2023) Corrigendum: Clinical features and gene variation analysis of COQ8B nephropathy: Report of seven cases. Front. Pediatr. 11:1183013. doi: 10.3389/fped.2023.1183013

Received: 9 March 2023; Accepted: 20 March 2023;
Published: 30 March 2023.

Approved by: Frontiers Editorial Office, Frontiers Media SA, Switzerland

© 2023 Liang, Chen, Zhang, Law, Yu, Jiao, Yang, Wu, Zhang, Chen, Wang, Yang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Anshuo Wang 181347201@qq.com

†These authors have contributed equally to this work and share first authorship

Specialty Section: This article was submitted to Children and Health, a section of the journal Frontiers in Pediatrics

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.